An overview of levodopa in the management of restless legs syndrome in a dialysis population: Pharmacokinetics, clinical trials, and complications oftherapy
L. Janzen et al., An overview of levodopa in the management of restless legs syndrome in a dialysis population: Pharmacokinetics, clinical trials, and complications oftherapy, ANN PHARMAC, 33(1), 1999, pp. 86-92
OBJECTIVE: To review published literature investigating the efficacy and sa
fety of levodopa. in the management of restless legs syndrome (RLS) with em
phasis on the hemodialysis population.
DATA SOURCES: An English-language literature search using MEDLINE was condu
cted from 1966 to 1997 (key terms. restless legs syndrome, levodopa, hemodi
alysis). The bibliographies of all identified published articles were revie
wed and cross-referenced to ensure that all possible references were identi
fied.
STUDY SELECTION AND DATA EXTRACTION: All identified human studies investiga
ting the use of levodopa for the management of RLS in uremic and nonuremic
patients were analyzed.
RESULTS: The prevalence of RLS is 20-40% in patients with end stage renal d
isease (ESRD) and approximately 5% in the general population. Although the
benefits of levodopa/(carbidopa/ benserazide) in reducing the signs and sym
ptoms of RLS are documented in nonuremic patients, evidence in patients wit
h ESRD is less readily available. Three small(<30 subjects) clinical trials
in uremic patients provide preliminary evidence for the usefulness of levo
dopa/(carbidopa/benserazide) in this population.
CONCLUSIONS: In general, the small amount of published literature supports
the empirical use of levodopa/carbidopa as a safe and effective therapy to
manage the distressing symptoms of RLS in a hemodialysis population. We als
o report personal observations over a 4-year period in our hemodialysis uni
t that support levodopa as an effective first-line therapy. We have averted
suicidal ideation in two patients and frequently modified symptoms of seve
re sleep deprivation. The dose of levodopa/carbidopa must be individually t
itrated to each patient's symptomatology, and morning rebound and afternoon
augmentation should be monitored.